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http://hub.abes.fr/acs/periodical/jmcmar/1992/volume_35/issue_11/101021jm00089a007/authorship/9
http://hub.abes.fr/acs/periodical/joceah/1995/volume_60/issue_6/101021jo00111a012/authorship/4
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http://hub.abes.fr/acs/periodical/joceah/1981/volume_46/issue_18/101021jo00331a005/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1990/volume_33/issue_8/101021jm00170a023/authorship/1
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Nucleosides. 104. Synthesis of 4-amino-5-(D-ribofuranosyl)pyrimidine C-nucleosides from 2-(2,3-O-isopropylidene-5-O-trityl-D-ribofuranosyl)acetonitrile
Nucleosides. 120. Syntheses of 2'-deoxy-.psi.-isocytidine and 2'-deoxy-1-methyl-.psi.-uridine from .psi.-uridine
Nucleosides. 123. Synthesis of antiviral nucleosides: 5-substituted 1-(2-deoxy-2-halogeno-.beta.-D-arabinofuranosyl)cytosines and -uracils. Some structure-activity relationships
Nucleosides. 98. Direct introduction of an acetamido group into the sugar moiety of nucleoside epoxides
Nucleosides. 116. 1-(.beta.-D-Xylofuranosyl)-5-fluorocytosines with a leaving group on the 3' position. Potential double-barreled masked precursors of anticancer nucleosides
Isolation of Compactin (A Hypocholestrolemic Metabolite) from a New Source: Penicillium cyclopium
Synthesis of enantiomerically pure (2'R,5'S)-(-)-1-(2-hydroxymethyloxathiolan-5-yl)cytosine as a potent antiviral agent against hepatitis B virus (HBV) and human immunodeficiency virus (HIV)
Conformational analysis of 2',3'-didehydro-2',3'-dideoxypyrimidine nucleosides
Nucleosides. 107. Synthesis of 5-(.beta.-D-arabinofuranosyl)isocytosine and related C-nucleosides
Brain targeting of anti-HIV nucleosides: synthesis and in vitro and in vivo studies of dihydropyridine derivatives of 3'-azido-2',3'-dideoxyuridine and 3'-azido-3'-deoxythymidine
Synthesis, Structure−Activity Relationships, and Drug Resistance ofβ-d-3‘-Fluoro-2‘,3‘-Unsaturated Nucleosides as Anti-HIV Agents
d- and l-2‘,3‘-Didehydro-2‘,3‘-dideoxy-3‘-fluoro-carbocyclic Nucleosides: Synthesis, Anti-HIVActivity and Mechanism of Resistance
Enantiomeric Syntheses of Conformationally Restricted d- andl-2‘,3‘-Dideoxy-2‘,3‘-endo-methylene Nucleosides fromCarbohydrate Chiral Templates
Synthesis of 3‘-Fluoro-2‘,3‘-dideoxy-2‘,3‘-didehydro-4‘-ethynyl-d-and -l-furanosyl Nucleosides
Synthesis of Cyclopentenyl Carbocyclic Nucleosides as Potential Antiviral Agents AgainstOrthopoxviruses and SARS
Structure−Activity Relationships of (E)-5-(2-Bromovinyl)uracil and RelatedPyrimidine Nucleosides as Antiviral Agents for Herpes Viruses
Synthesis and Anti-HIV Activity of d- and l-Thietanose Nucleosides
Stereoselective Synthesis and Antiviral Activity ofd-2‘,3‘-Didehydro-2‘,3‘-dideoxy-2‘-fluoro-4‘-thionucleosides
Synthesis, Antiviral Activity, and Mechanism of Drug Resistance of d- andl-2‘,3‘-Didehydro-2‘,3‘-dideoxy-2‘-fluorocarbocyclic Nucleosides
PracticalSynthesis of d- and l-2-Cyclopentenone and Their Utility for theSynthesis of Carbocyclic Antiviral Nucleosides against OrthopoxViruses (Smallpox, Monkeypox, and Cowpox Virus).
Stereocontrolled Syntheses of Carbocyclic C-Nucleosides andRelated Compounds
Enantiomeric Synthesis of d- and l-Cyclopentenyl Nucleosides and TheirAntiviral Activity Against HIV and West Nile Virus
Practical Synthesis of d- and l-2-Cyclopentenone and Their Utilityfor the Synthesis of Carbocyclic Antiviral Nucleosides againstOrthopox Viruses (Smallpox, Monkeypox, and Cowpox Virus)
Synthesis and Antiviral Activity of Oxaselenolane Nucleosides
Structure−Activity Relationships of 7-Deaza-6-benzylthioinosine Analogues as Ligands of Toxoplasma gondii Adenosine Kinase
Synthesis and antiviral activity of various 3'-azido analogs of pyrimidine deoxyribonucleosides against human immunodeficiency virus (HIV-1, HTLV-III/LAV)
Synthesis and structure-activity relationships of 6-substituted 2',3'-dideoxypurine nucleosides as potential anti-human immunodeficiency virus agents
Enhanced Brain Delivery of an Anti-HIV Nucleoside 2'-F-ara-ddI by Xanthine Oxidase Mediated Biotransformation
Asymmetric synthesis of 1,3-dioxolane-pyrimidine nucleosides and their anti-HIV activity.
1,3-Dioxolanylpurine nucleosides (2R,4R) and (2R,4S) with selective anti-HIV-1 activity in human lymphocytes
Structure-activity relationships of pyrimidine nucleosides as antiviral agents for human immunodeficiency virus type 1 in peripheral blood mononuclear cells
Structure-activity relationships of .beta.-D-(2S,5R)- and .alpha.-D-(2S,5S)-1,3-oxathiolanyl nucleosides as potential anti-HIV agents
L-.beta.-(2S,4S)- and L-.alpha.-(2S,4R)-dioxolanyl nucleosides as potential anti-HIV agents: asymmetric synthesis and structure-activity relationships
Asymmetric synthesis and biological evaluation of .beta.-L-(2R,5S)- and .alpha.-L-(2R,5R)-1,3-oxathiolane-pyrimidine and -purine nucleosides as potential anti-HIV agents
Hybrid Pharmacokinetic Models to Describe Anti-HIV Nucleoside Brain Disposition Following Parent and Prodrug Administration in Mice
Asymmetric Synthesis of (1'S,2'R)-Cyclopropyl Carbocyclic Nucleosides
Nucleosides. 100. General synthesis of pyrimidine C-5 nucleosides related to pseudouridine. Synthesis of 5-(.beta.-D-ribofuranosyl)isocytosine (pseudoisocytidine), 5-(.beta.-D-ribofuranosyl)-2-thiouracil (2-thiopseudouridine), and 5-(.beta.-D-ribofuranosyl)uracil (pseudouridine)
Synthesis of L-Dioxolane Nucleosides and Related Chemistry
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